|Publication number||US7749279 B2|
|Application number||US 10/564,130|
|Publication date||Jul 6, 2010|
|Filing date||Dec 5, 2003|
|Priority date||Dec 7, 2002|
|Also published as||DE60326751D1, EP1567095A1, EP1567095B1, US20070083212, WO2004052243A1|
|Publication number||10564130, 564130, PCT/2003/5324, PCT/GB/2003/005324, PCT/GB/2003/05324, PCT/GB/3/005324, PCT/GB/3/05324, PCT/GB2003/005324, PCT/GB2003/05324, PCT/GB2003005324, PCT/GB200305324, PCT/GB3/005324, PCT/GB3/05324, PCT/GB3005324, PCT/GB305324, US 7749279 B2, US 7749279B2, US-B2-7749279, US7749279 B2, US7749279B2|
|Inventors||Richard Twomey, Neil Watkins, Rick Kowalski, John Ewans|
|Original Assignee||Depuy International Ltd.|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (18), Referenced by (28), Classifications (33), Legal Events (2)|
|External Links: USPTO, USPTO Assignment, Espacenet|
This invention relates to a bone cement plug for fitting into the intramedullary canal within a bone to restrict flow of bone cement during surgery.
Surgical procedures in which components of orthopaedic joint prostheses are fixed to natural bone tissue by means of curable bone cement materials are well established. Components which are to be fixed to a long bone such as the femoral component of a hip joint prosthesis or the humeral component of a shoulder joint prosthesis have a stem which is received in the intramedullary canal of the bone, which is fixed within the canal by means of bone cement. The surgical procedure generally involves injecting a quantity of bone cement into the canal prior to locating the stem of the prosthesis into the canal so as to apply pressure to the cement. The cement is then allowed to cure.
It can be important to limit the depth within the canal into which the cement penetrates, for example to minimise undesirable effects in other parts of the patient's bone structure, and also significantly to enable pressure to be applied to the cement when the prosthesis component is implanted, to encourage the cement to penetrate the wall of the bone which defines the intramedullary cavity. It is known to use a bone cement plug in order to define the distal end of the cavity into which the stem of a prosthesis component is to be implanted, to limit the depth within the canal into which cement can penetrate. The bone cement plug should engage the wall of the canal so that it is not displaced significantly when the stem of the prosthesis component is inserted into the canal. Generally, the bone cement plug is prevented from being displaced by frictional forces between it and the internal wall of the canal. Proper selection of a bone cement plug which has an appropriate size to be an interference fit in the canal is essential: if the bone cement plug is too big, either it or the bone tissue which defines the canal will be damaged, and if it is too small, it will not engage the internal wall of the cavity with sufficient security for it to be displaced when the bone cement is pressurised.
Bone cement plugs which can be expanded transversely to engage the wall of the intra-medullary canal are known. For example, a bone cement plug is disclosed in WO-00/28926 which comprises a quantity of a deformable plugging material which is located between two plates. An instrument is included by which one of the plates can be drawn towards the other plate, compressing the plugging material axially and causing its transverse dimension to increase to engage the wall of the intramedullary canal. A bone cement plug is disclosed in U.S. Pat. No. 4,447,915 which comprises a hollow outer member and a conical expander. The outer member can be expanded transversely by drawing the expander into the outer member.
It can be desirable for a bone cement plug to have a wide range of expansion so that it can be used in patient's bones with a wide range of sizes of intramedullary canal. The present invention provides a bone cement plug which comprises a hollow sleeve having a cavity within it and whose wall thickness increases towards one end, and an expander which can be drawn into the cavity, towards the end of the sleeve in a direction from the end with the smaller wall thickness towards the end with the larger wall thickness.
Accordingly, in one aspect, the invention provides a bone cement plug for fitting into the intramedullary canal within a bone to restrict flow of bone cement during surgery, which comprises:
The bone cement plug of the invention has the advantage that it can be expanded to engage the internal surfaces of the intramedullary cavity within bones with a wide range of sizes, with sufficiently secure interference fits for the plug to remain approximately in place even when subjected to the pressures which can result from the insertion into the cavity of the stem of a prosthesis component. This arises from the convergence of the inner surfaces of the sleeve wall.
Preferably, the sleeve has an end wall at the end towards which the expander is drawn to cause the sleeve to expand. The end wall can be formed as a single body (usually of the same material) with the wall of the sleeve which contacts the surface of the canal when the sleeve is expanded.
Preferably, the end wall of the sleeve has an opening extending through it. Preferably, the expander comprises a shaft which extends generally along the sleeve axis, and a transverse portion which contacts the internal wall of the cavity in the sleeve, the shaft extending through the opening in the end wall of the sleeve to that it can be engaged to draw the expander through the sleeve.
Preferably, the shaft has a line of weakness at which it can be broken to allow the transverse portion of the expander to be separated from that portion of the shaft which extends through the opening in the end wall of the sleeve. It will generally be preferred that the line of weakness is positioned so that the shaft does not protrude significantly through the opening in the sleeve when the sleeve has been expanded to contact the patient's bone tissue.
Preferably, the expander includes a conical washer on the shaft which sits on the transverse portion of the expander. It is particularly preferred that the conical washer has a plurality of slots formed in it, extending partially from the outside edge of the washer towards the inside edge thereof. The slots can extend radially. The use of a conical washer has been found to increase the range of sizes to which the sleeve can be expanded. The slots allow the washer to be deformed from a conical configuration towards a flattened configuration, as the expander is drawn into the cavity within the sleeve, increasing the transverse dimension of the washer, and therefore also the effective transverse dimension of the expander.
Preferably, the shaft and transverse portion of the expander are moulded as a single component. The shaft and the transverse portion of the expander can be formed from a resorbable material, for example by moulding. The shaft and the transverse portion can be formed from a material which can be used as a bone cement, for example a polymethyl-methacrylate. The material from which the shaft and transverse portion are made should be stiffer than the material of the sleeve so that it is the sleeve which is deformed primarily when the expander is drawn into the cavity in the sleeve. The washer (when present) can be made from a material which is different from that of the shaft and the transverse portion, especially when the washer is required to deform during deformation of the sleeve.
The angle between the inner surface of the wall and the axis of the sleeve, at the end of the sleeve from which the expander is drawn through the cavity in a direction to cause the sleeve to expand transversely, will be selected so that the transverse dimension of the sleeve can be made to increase without the need to draw the expander a significant distance into the cavity within the sleeve. However, the angle should not be so great that there is significant resistance to the expander being drawn into the sleeve. Preferably, the angle between the inner surface of the wall and the axis of the sleeve, at the end of the sleeve from which the expander is drawn through the cavity in a direction to cause the sleeve to expand transversely, is at least about 20°, more preferably at least about 25°. Preferably, the angle between the inner surface of the wall and the axis of the sleeve, at the end of the sleeve from which the expander is drawn through the cavity in a direction to cause the sleeve to expand transversely, is not more than about 50°, more preferably not more than about 40°.
The outer surface of the sleeve can have surface features to promote engagement with the bone surface of the intramedullary canal. For example, the outer surface can be roughened, or it can have ridges or grooves or both on it extending in a plane generally perpendicular to the axis of the sleeve. Surface features can increase frictional forces between the sleeve and the inner surface of the intramedullary cavity.
The sleeve can have one or more indents in the surface which defines the internal cavity, extending around the cavity approximately in a plane which is perpendicular to the axis of the sleeve. Such an indent can promote engagement of the expander with the inner surface to minimise the risk of the sleeve relaxing from its expanded configuration.
The material of the sleeve should be selected having regard to its deformability. The material should be capable of being deformed by the application of moderate force to the expander. However, it has been found that materials which can be deformed too easily tend to compress in the direction in which the expander is moved in order to cause the sleeve to expand. Preferably, the hardness of the material of the sleeve is at least about 15 Shore A, more preferably at least about 20 Shore A, especially at least about 25 Shore A. Preferably, the hardness of the material of the sleeve is not more than about 75 Shore A, more preferably not more than about 55 Shore A, especially not more than about 40 Shore A. The deformability of the sleeve enables it to be expanded to fit into bone canals with a range of sizes. It can also enable it to deform to change its cross-sectional shape, for example from circular when the cross-sectional shape of the bone canal is not circular.
It can be preferred for many applications for the material of the sleeve to be resorbable. Examples of suitable resorbable materials include materials containing one or more of gelatine, glycerol, polyethylene oxide, polyethylene glycol/polybutylene terephthalate copolymer, and a foamed polylactide polymer (PLLA). Non-resorbable materials can be used such as certain elastomers. A preferred example is based on a polyurethane.
For some applications, it can be preferred for part only of the sleeve to be resorbable, for example by forming the sleeve in two or more layers of which one or more can be resorbed. In this way, partial resorption of the material of the sleeve can reduce pressure on the bone tissue which defines the intramedullary cavity. The resorbable layer can be an inner layer. Preferably, it is an outer layer.
In another aspect, the invention provides an assembly for use in orthopaedic surgery which comprises a bone cement plug as discussed above and an instrument for locating the plug in the intramedullary canal within a bone.
Preferably, the expander comprises a shaft which extends generally along the sleeve axis, and the instrument includes a socket for engaging the shaft on the expander. Preferably, the assembly includes a drive unit by which the expander can be drawn into the sleeve to cause it to expand transversely. The drive unit can be operated manually, preferably with a ratchet mechanism which allows for progressive and controlled drawing of the expander into the sleeve cavity. When the shaft has a line of weakness, continued controlled drawing the expander into sleeve cavity can lead to breakage of the shaft. The instrument for drawing the expander can be of the kind disclosed in WO-00/28926.
Embodiments of the present invention will now be described by way of example with reference to the accompanying drawings, in which:
Referring to the drawings,
The bone cement plug is formed as a sleeve from a material which is capable of being expanded transversely. A preferred material for the expander is based on an ethylene oxide/polybutylene terephthalate copolymer. The material should be compounded so that its hardness, measured on the Shore A scale, is between about 25 and about 40.
The sleeve of the bone cement plug comprises an axially extending side wall whose outer surface 10 has an approximately constant cross-sectional shape and size. The cross-sectional shape of outer surface will generally be approximately circular. The sleeve is hollow, having a cavity 12 defined by an inner wall which converges from an open end 14 to a closed end 16. The sleeve has an end wall at the closed end, which has an opening 18 extending through it through which the shaft 4 of the expander can slide. The sleeve can be formed by techniques such as moulding and machining.
The angle α between the outer surface 10 of the sleeve and the inner wall which defines the cavity 12 is about 30°.
The expander comprises a shaft 4 and a transverse portion 6 at the base of the shaft. The shaft and the transverse portion are formed as a single part by an injection moulding process. It is generally preferred that they are formed from a material which can be used as a bone cement, such as cured polymethylmethacrylate. The shaft has a line of weakness formed in it, close to its base, provided by a groove 20. The shaft has a recess 22 close to the end opposite the base, by which the shaft can be engaged by an instrument for locating the plug in an intramedullary canal.
The expander includes a conical washer 8 which has an opening 24 extending through it through which the shaft can extend so that the washer sits against the transverse portion 6 of the expander. The washer has a plurality of slots formed in it, extending radially from the outer edge of the washer towards its centre. The slots enable the washer to be deformed from its conical configuration towards a flattened configuration so that the diameter of the washer increases. The diameter of the washer prior to it being deformed is about the same as the diameter of the transverse portion of the expander. Once it has been deformed, the diameter of the washer is greater than the diameter of the transverse portion of the expander.
A bone is prepared to receive the bone cement plug by appropriate resection of the diseased or otherwise damaged tissue. The exposed intramedullary cavity is prepared using appropriate cutting tools such as reamers and broaches, so that the cavity in the region in which the stem of a prosthesis component is to extend is defined by cancellous tissue, and so that the cross-section of the canal is circular or close to circular.
The bone cement plug, when prepared for implantation in a bone canal, is assembled as shown in
The instrument is used to insert the bone cement plug into the prepared canal at the appropriate depth so that the stem of the prosthesis component can fit into the canal. The instrument is then actuated to draw the expander through the sleeve 2, relying on the engagement between grip means on the instrument and the recess on the shaft. This causes the transverse portion 2 of the expander and the washer 8 to be drawn into the cavity 12 within the sleeve. The reducing diameter of the cavity and the action of the transverse portion against it, causes the sleeve to be deformed outwardly, to engage the inner surface 32 of the bone canal. Continued drawing of the expander into the sleeve causes the washer to flatten, so that its diameter increases as shown in
When the force required to deform the sleeve on continued displacement of the expander through the cavity, reaches a certain level, it causes the shaft to break at the line of weakness provided by the groove 20. The shaft can be configured so that it breaks under a predetermined axial load. The shaft can then be removed from within the bone canal. The expanded sleeve remains within the canal, with the transverse portion of the expander and the washer within it. The short portion of the shaft above the transverse portion is located wholly within the sleeve (as shown in
Examples of dimensions (in millimetres) of bone cement plugs according to the invention are as follows:
Overall length of sleeve (2)
Diameter of sleeve (2)
Diameter of opening(18) in sleeve
Wall thickness of sleeve at open end (14)
Wall thickness of sleeve at closed end (16)
Length of shaft (4)
Diameter of transverse portion (6)
Diameter of conical washer -
Height of conical washer - undeformed
Minimum diameter of bone canal
Maximum diameter of bone canal
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US4011602 *||Oct 6, 1975||Mar 15, 1977||Battelle Memorial Institute||Porous expandable device for attachment to bone tissue|
|US4447915 *||Feb 3, 1982||May 15, 1984||Sulzer Brothers Limited||Expandable medullary canal plug|
|US5092891||Mar 8, 1990||Mar 3, 1992||Kummer Frederick J||Cement plug for the medullary canal of a bone and coacting tool for installing same|
|US5554191 *||Jan 23, 1995||Sep 10, 1996||Biomat||Intersomatic vertebral cage|
|US5935169 *||Feb 13, 1997||Aug 10, 1999||Chan; Kwan-Ho||Bone cement plug for deployment in a bone canal|
|US5997580 *||May 6, 1997||Dec 7, 1999||Johnson & Johnson Professional, Inc.||Cement restrictor including shape memory material|
|US6123706 *||Dec 17, 1998||Sep 26, 2000||Lange; Robert||Apparatus for stabilizing certain vertebrae of the spine|
|US6669733 *||Nov 12, 1999||Dec 30, 2003||Petrus Tarasius Josephus Spierings||Bone plug|
|US7156880 *||Aug 14, 2003||Jan 2, 2007||Kensey Nash Corporation||Devices and methods for treating defects in the tissue of a living being|
|US20030065395 *||Jun 21, 2002||Apr 3, 2003||Ralph James D.||Artificial intervertebral disc having a slotted belleville washer force restoring element|
|DE3445709A1||Dec 14, 1984||Jun 19, 1986||Draenert Klaus||Verschluss aus chirurgischem material|
|DE4439049A1||Nov 2, 1994||Jul 11, 1996||Corimed Kundenorientierte Medi||Method and device for closing medulla of femur during implantation of prosthesis|
|FR2708192A1||Title not available|
|GB2253564A||Title not available|
|GB2324731A||Title not available|
|WO2000024341A2||Oct 21, 1999||May 4, 2000||Pierson Raymond H Iii||Bone canal plug and method of making|
|WO2000026926A1||Oct 25, 1999||May 11, 2000||Santoku America, Inc.||Sm(Co, Fe, Cu, Zr, C) COMPOSITIONS AND METHODS OF PRODUCING SAME|
|WO2001066045A1||Mar 9, 2000||Sep 13, 2001||Coripharm Medizinprodukte Gmbh & Co. Kg||Device for closing the medullary space of the femur used for endoprosthetic implants|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US8088163||Feb 6, 2009||Jan 3, 2012||Kleiner Jeffrey B||Tools and methods for spinal fusion|
|US8277510||Oct 20, 2011||Oct 2, 2012||Kleiner Intellectual Property, Llc||Tools and methods for spinal fusion|
|US8292918 *||Feb 20, 2009||Oct 23, 2012||Boston Scientific Scimed, Inc.||Composite plug for arteriotomy closure and method of use|
|US8292960||May 16, 2012||Oct 23, 2012||Kleiner Intellectual Property, Llc||Spinal fusion cage with removable planar elements|
|US8366748||Dec 7, 2009||Feb 5, 2013||Kleiner Jeffrey||Apparatus and method of spinal implant and fusion|
|US8632603||Sep 21, 2010||Jan 21, 2014||Tornier, Inc.||Implant positioning systems for orienting prosthesis|
|US8685031||Jul 22, 2013||Apr 1, 2014||Spinal Surgical Strategies, Llc||Bone graft delivery system|
|US8709088||Nov 22, 2013||Apr 29, 2014||Spinal Surgical Strategies, Llc||Fusion cage with combined biological delivery system|
|US8715355||Oct 22, 2012||May 6, 2014||Nuvasive, Inc.||Spinal fusion cage with removable planar elements|
|US8808305||Oct 1, 2012||Aug 19, 2014||Jeffrey B. Kleiner||Spinal fusion cage system with inserter|
|US8864654||Apr 20, 2011||Oct 21, 2014||Jeffrey B. Kleiner||Method and apparatus for performing retro peritoneal dissection|
|US8870882||Jan 30, 2013||Oct 28, 2014||Jeffrey KLEINER||Apparatus and method of spinal implant and fusion|
|US8906028||Sep 20, 2010||Dec 9, 2014||Spinal Surgical Strategies, Llc||Bone graft delivery device and method of using the same|
|US9060877||Feb 6, 2012||Jun 23, 2015||Spinal Surgical Strategies, Llc||Fusion cage with combined biological delivery system|
|US9173694||Dec 14, 2012||Nov 3, 2015||Spinal Surgical Strategies, Llc||Fusion cage with combined biological delivery system|
|US9186193||Apr 28, 2014||Nov 17, 2015||Spinal Surgical Strategies, Llc||Fusion cage with combined biological delivery system|
|US9216046||Apr 10, 2012||Dec 22, 2015||Joseph P. Iannotti||Methods and devices for bone preparation|
|US9247943||Jun 24, 2011||Feb 2, 2016||Kleiner Intellectual Property, Llc||Devices and methods for preparing an intervertebral workspace|
|US9427264||Oct 6, 2014||Aug 30, 2016||Jeffrey KLEINER||Apparatus and method of spinal implant and fusion|
|US9439782||Aug 18, 2014||Sep 13, 2016||Jeffrey B. Kleiner||Spinal fusion cage system with inserter|
|US20100217312 *||Feb 20, 2009||Aug 26, 2010||Boston Scientific Scimed, Inc.||Composite plug for arteriotomy closure and method of use|
|US20130312762 *||Aug 3, 2012||Nov 28, 2013||Nandhika Wijay||Reversible Acute Occlusion Implant, Delivery Catheter and Method|
|USD656610||Jun 8, 2011||Mar 27, 2012||Kleiner Jeffrey B||Spinal distraction instrument|
|USD667542||Mar 14, 2012||Sep 18, 2012||Kleiner Jeffrey B||Spinal distraction instrument|
|USD696399||Sep 28, 2012||Dec 24, 2013||Kleiner Intellectual Property, Llc||Spinal distraction instrument|
|USD700322||Jul 17, 2012||Feb 25, 2014||Jeffrey B. Kleiner||Intervertebral surgical tool|
|USD723682||May 3, 2013||Mar 3, 2015||Spinal Surgical Strategies, Llc||Bone graft delivery tool|
|USD750249||Oct 20, 2014||Feb 23, 2016||Spinal Surgical Strategies, Llc||Expandable fusion cage|
|International Classification||A61F2/30, A61F2/44, A61F2/46, A61F2/00, A61F2/02|
|Cooperative Classification||A61F2/30771, A61F2310/00353, A61F2002/30062, A61F2002/30822, A61F2002/30598, A61F2002/30561, A61F2002/4631, A61F2002/30604, A61F2230/0069, A61F2002/30957, A61F2002/30487, A61F2002/30929, A61F2002/30372, A61F2/4614, A61F2210/0004, A61F2002/30233, A61F2002/30579, A61F2220/0033, A61F2/30723, A61F2002/30069, A61F2240/004, A61F2002/30064, A61F2002/30514, A61F2220/0025, A61F2250/0071|
|European Classification||A61F2/30B1, A61F2/46B9|
|Sep 8, 2006||AS||Assignment|
Owner name: DEPUY INTERNATIONAL, LTD., UNITED KINGDOM
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:TWOMEY, RICHARD;WATKINS, NEIL;KOWALSKI, RICK;AND OTHERS;REEL/FRAME:018220/0135;SIGNING DATES FROM 20060704 TO 20060710
Owner name: DEPUY INTERNATIONAL, LTD., UNITED KINGDOM
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:TWOMEY, RICHARD;WATKINS, NEIL;KOWALSKI, RICK;AND OTHERS;SIGNING DATES FROM 20060704 TO 20060710;REEL/FRAME:018220/0135
|Dec 11, 2013||FPAY||Fee payment|
Year of fee payment: 4